NP001 regulation of macrophage activation markers in ALS: A phase I clinical and biomarker study

被引:40
作者
Miller, Robert G. [1 ]
Zhang, Rongzhen [2 ]
Block, Gilbert [3 ]
Katz, Jonathan [1 ]
Barohn, Richard [4 ]
Kasarskis, Edward [5 ]
Forshew, Dallas [1 ]
Gopalakrishnan, Vidhya [3 ]
McGrath, Michael S. [2 ,3 ]
机构
[1] Calif Pacific Med Ctr, San Francisco, CA USA
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
[3] Neuraltus Pharmaceut Inc, Palo Alto, CA USA
[4] Univ Kansas, Med Ctr, Res Inst, Kansas City, KS USA
[5] Univ Kentucky, ALS Ctr, Kentucky Neurosci Inst, Lexington, KY 40506 USA
关键词
NP001; ALS; inflammation; monocyte; macrophage; AMYOTROPHIC-LATERAL-SCLEROSIS; MONOCYTE CHEMOATTRACTANT PROTEIN-1; CIRCULATING MONOCYTES; INFLAMMATORY MECHANISMS; CD16(+) MONOCYTES; IMMUNE; DISEASE; CELLS; INFECTION; DEMENTIA;
D O I
10.3109/21678421.2014.951940
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This is a phase I, placebo-controlled, single ascending dose safety and tolerability study of NP001 in patients with ALS. NP001 is a novel regulator of inflammatory macrophages and monocytes. As ALS progression is thought to be related to neuroinflammation, an additional objective of the study was to assess the effects of NP001 administration on monocyte activation markers. Thirty-two ALS patients were enrolled and received either placebo (eight) or one of four (six at each dose) ascending single i.v. doses (0.2, 0.8, 1.6 and 3.2 mg/kg NP001). Patients were monitored for safety, and blood monocyte immune activation markers CD16 and HLA-DR were assessed pre- and 24 h post-dosing. Changes from baseline were calculated. Results showed that NP001 was generally safe and well tolerated. Importantly, a single dose of NP001 caused a dose-dependent reduction in expression of monocyte CD16, a marker of monocyte activation/inflammation. Additionally, monocyte HLA-DR expression was also decreased in those patients with elevated values at baseline. In conclusion, these data indicate that NP001 has an acute effect on inflammatory monocytes in ALS patient blood. The potential for modulation of inflammation in the context of ALS disease progression will require further study with long-term follow-up.
引用
收藏
页码:601 / 609
页数:9
相关论文
共 53 条
  • [1] Optineurin suppression causes neuronal cell death via NF-κB pathway
    Akizuki, Mayumi
    Yamashita, Hirofumi
    Uemura, Kengo
    Maruyama, Hirofumi
    Kawakami, Hideshi
    Ito, Hidefumi
    Takahashi, Ryosuke
    [J]. JOURNAL OF NEUROCHEMISTRY, 2013, 126 (06) : 699 - 704
  • [2] Transendothelial migration of CD16+ monocytes in response to fractalkine under constitutive and inflammatory conditions
    Ancuta, P
    Moses, A
    Gabuzda, D
    [J]. IMMUNOBIOLOGY, 2004, 209 (1-2) : 11 - 20
  • [3] CD16+ monocytes produce IL-6, CCL2, and matrix metalloproteinase-9 upon interaction with CX3CL1-expressing endothelial cells
    Ancuta, Petronela
    Wang, Jianbin
    Gabuzda, Dana
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 2006, 80 (05) : 1156 - 1164
  • [4] Elevated inflammatory markers in a group of amyotrophic lateral sclerosis patients from Northern India
    Babu, G. Nagesh
    Kumar, Alok
    Chandra, Ramesh
    Puri, S. K.
    Kalita, Jayantee
    Misra, U. K.
    [J]. NEUROCHEMICAL RESEARCH, 2008, 33 (06) : 1145 - 1149
  • [5] Adaptive Immune Neuroprotection in G93A-SOD1 Amyotrophic Lateral Sclerosis Mice
    Banerjee, Rebecca
    Mosley, R. Lee
    Reynolds, Ashley D.
    Dhar, Alok
    Jackson-Lewis, Vernice
    Gordon, Paul H.
    Przedborski, Serge
    Gendelman, Howard E.
    [J]. PLOS ONE, 2008, 3 (07):
  • [6] Motor neuron-immune interactions: the vicious circle of ALS
    Barbeito, Ana G.
    Mesci, Pinar
    Boillee, Severine
    [J]. JOURNAL OF NEURAL TRANSMISSION, 2010, 117 (08) : 981 - 1000
  • [7] Production of monocyte chemoattractant protein-1 in amyotrophic lateral sclerosis
    Baron, P
    Bussini, S
    Cardin, V
    Corbo, M
    Conti, G
    Galimberti, D
    Scarpini, E
    Bresolin, N
    Wharton, SB
    Shaw, PJ
    Silani, V
    [J]. MUSCLE & NERVE, 2005, 32 (04) : 541 - 544
  • [8] CD4+T cells support glial neuroprotection, slow disease progression, and modify glial morphology in an animal model of inherited ALS
    Beers, David R.
    Henkel, Jenny S.
    Zhao, Weihua
    Wang, Jinghong
    Appel, Stanley H.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (40) : 15558 - 15563
  • [9] The proinflammatory CD14+CD16+DR++ monocytes are a major source of TNF
    Belge, KU
    Dayyani, F
    Horelt, A
    Siedlar, M
    Frankenberger, M
    Frankenberger, B
    Espevik, T
    Ziegler-Heitbrock, L
    [J]. JOURNAL OF IMMUNOLOGY, 2002, 168 (07) : 3536 - 3542
  • [10] ALS:: A disease of motor neurons and their nonneuronal neighbors
    Boillee, Sverine
    Vande Velde, Christine
    Cleveland, Don W.
    [J]. NEURON, 2006, 52 (01) : 39 - 59